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Q47827561-22F0EB48-D857-485C-844D-7057721DF48B
Q47827561-22F0EB48-D857-485C-844D-7057721DF48B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47827561-22F0EB48-D857-485C-844D-7057721DF48B
Multiple clinical profiles of families with the short QT syndrome.
P2860
Q47827561-22F0EB48-D857-485C-844D-7057721DF48B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47827561-22F0EB48-D857-485C-844D-7057721DF48B
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1a3b7c9f43d15d59ea4750fbf78b995f16e98bbf
P2860
A novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 gene